Lumiflavin

Lumiflavin
Names
Preferred IUPAC name
7,8,10-Trimethylbenzo[g]pteridine-2,4(3H,10H)-dione
Other names
Lumilactoflavin
Identifiers
CAS Number
  • 1088-56-8 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:43661 checkY
ChemSpider
  • 59571 checkY
DrugBank
  • DB04726 checkY
ECHA InfoCard 100.012.841 Edit this at Wikidata
PubChem CID
  • 66184
UNII
  • 4M2669414M checkY
CompTox Dashboard (EPA)
  • DTXSID10148745 Edit this at Wikidata
InChI
  • InChI=1S/C13H12N4O2/c1-6-4-8-9(5-7(6)2)17(3)11-10(14-8)12(18)16-13(19)15-11/h4-5H,1-3H3,(H,16,18,19) checkY
    Key: KPDQZGKJTJRBGU-UHFFFAOYSA-N checkY
  • InChI=1/C13H12N4O2/c1-6-4-8-9(5-7(6)2)17(3)11-10(14-8)12(18)16-13(19)15-11/h4-5H,1-3H3,(H,16,18,19)
    Key: KPDQZGKJTJRBGU-UHFFFAOYAD
  • O=C2/N=C\1/N(c3cc(c(cc3/N=C/1C(=O)N2)C)C)C
Properties
Chemical formula
C13H12N4O2
Molar mass 256.265 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references
Chemical compound

Lumiflavin is a toxic product of photolysis of vitamin B2.[1]

References

  1. ^ Rodríguez-Otero, Jesús; Martínez-Núñez, Emilio; Peña-Gallego, Angeles; Vázquez, Saulo A (2002). "The Role of Aromaticity in the Planarity of Lumiflavin". The Journal of Organic Chemistry. 67 (18): 6347–6352. doi:10.1021/jo011159c. PMID 12201752.
  • v
  • t
  • e